The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
The formation of afferent patterns in the somatosensory cortex of the neonatal rat
Abstract
In the rat, the clustered pattern of thalamocortical afferent terminals to the “barrel field” portion of primary somatosensory cortex replicates the arrangement of vibrissae on the face, and the pattern of the terminals can be altered by the removal of vibrissae at birth (Killackey et al., 1976). These patterns of terminals were studied using the enzyme succinic dehydrogenase (SDH) because in somatosensory cortex the activity levels of SDH closely correspond to the patterns of thalamocortical afferent terminals. The present experiments show that the pattern of high SDH segmentation in the portion of layer IV of somatosensory cortex that is related to the vibrissae develops during postnatal Days 3 through 6. Activity related to the centers of individual clusters is first visible, with indistinct boundaries. At later times the edges of individual clusters become apparent. Further, in animals with Row C of vibrissae removed at birth, the abnormal SDH segmentation in somatosensory cortex develops with a time course similar to that of normal animals. At ages when edge boundaries are first distinct, a fused band corresponding to the removed row of vibrissae is present. Thus the aberrant organization seen in the adult cortex is the result of an abnormal initial development, not a later reorganization from a normal pattern. And indeed, vibrissae removal at Day 5 or 6 does not result in an aberrant cortical SDH pattern. Finally, after removal of all five rows of mystacial vibrissae at birth, the cortical SDH pattern seen at postnatal Days 6 and 7 consists of five bands in place of the normally present five rows of clusters. This may indicate that closer relationships exist between vibrissae within one row than vibrissae in adjacent rows.
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Citations
Cites
The period of susceptibility to the physiological effects of unilateral eye closure in kittens
Hubel, D. H., & Wiesel, T. N. (1970) · The Journal of Physiology · doi:10.1113/jphysiol.1970.sp009022 · Cited by 3,030
Rate and extent of recovery from dark rearing in the visual cortex of the mouse
Valverde, F. (1971) · Brain Research · doi:10.1016/0006-8993(71)90302-7 · Cited by 235
Mouse SmI cortex: qualitative and quantitative classification of golgi-impregnated barrel neurons.
Woolsey, T. A., Dierker, M. L., & Wann, D. F. (1975) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.72.6.2165 · Cited by 203
Cited by
Wong-Riley, M. T., & Welt, C. (1980) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.77.4.2333 · Cited by 462
Shatz, C., & Luskin, M. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-12-03655.1986 · Cited by 326
Anatomical pathways and molecular mechanisms for plasticity in the barrel cortex
Fox, K. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00027-1 · Cited by 310
Jensen, K., & Killackey, H. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-11-03529.1987 · Cited by 276
Self-citationAgmon, A., Yang, L., O'Dowd, D., & Jones, E. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-12-05365.1993 · Cited by 268
Metadata
- Authors
- Killackey, H. P., & Belford, G. R.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1979-01-15
- Volume
- 183
- Issue
- 2
- Pages
- 285-303
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W1968227329
- Cited by
- 287
- References
- 3
- FWCI
- 8.29
- Type
- journal article
- Language
- en
- Open access
- closed
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